A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671505



Internal ID9590924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63672102..63674386hg38UCSC Ensembl
chr17:61749462..61751746hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6081610
SamplesNA19468
Known GenesMAP3K3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671505
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer